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Sacral Erector Spinae Plane Block in Normal Birth

StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗
Record status
This record was last updated October 8, 2024 (before its estimated September 15, 2025 completion). Its status may not reflect the trial's current state.

Record History

  1. Primary completion date: Sep 15, 2024 to Sep 15, 2025
    • Study completion date: Nov 15, 2024 to Nov 15, 2025
    v6
  2. Primary completion date: Jul 15, 2024 to Sep 15, 2024
    • Study completion date: Jul 15, 2024 to Nov 15, 2024
    v5
  3. Primary and study completion dates: Jun 15, 2024 to Jul 15, 2024v4
  4. Primary completion date: May 1, 2024 to Jun 15, 2024
    • Study completion date: Jun 1, 2024 to Jun 15, 2024
    v3
  5. Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 1
    • Start date changed from estimate of Feb 1, 2024 to Jan 24, 2024
    v2
  6. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Pregnant women feel severe pain during normal birth and in the postpartum period. Preventing pain during and after birth is very important for both the mother and the baby. Rapid recovery in the postoperative period in pregnant women is very important for both mother and baby. To evaluate this recovery, the quality of recovery-10 scores developed by Shalev et al. are used in pregnant women. Our study will be the first in the literature to use sacral erectör spinae plane block (S-ESPB) in normal birth. Our primary aim in this study is to evaluate the effects of S-ESPB on the quality of recovery and recovery at the 24th hour in pregnant women who will undergo vaginal birth with epidural analgesia, using the Quality of Recovery-10T scores.
Trial Details
NCT Number NCT06221332
Lead Sponsor Konya City Hospital
Conditions
(from sponsor)		 Analgesia
Related terms Agnosia
Enrollment 40 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov